Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Janet Chou

Showing results (41-50 of 152) with videos related to

Pageof 16
Sort By:
Clinical Immunology (Orlando, Fla.)|August 20, 2016
Mutations in pyrin masquerading as a primary immunodeficiencyYousef R Badran, Mariam Rajab, Rima Hanna-Wakim, et al.
Clinical Immunology (Orlando, Fla.)|August 21, 2017
Combined immunodeficiency with EBV positive B cell lymphoma and epidermodysplasia verruciformis due to a novel homozygous mutation in RASGRP1Craig D Platt, Ari J Fried, Rodrigo Hoyos-Bachiloglu, et al.
Clinical Immunology (Orlando, Fla.)|April 12, 2016
Combined immunodeficiency due to a homozygous mutation in ORAI1 that deletes the C-terminus that interacts with STIM 1Yousef R Badran, Michel J Massaad, Wayne Bainter, et al.
The Journal of Experimental Medicine|June 11, 2017
Human <i>RELA</i> haploinsufficiency results in autosomal-dominant chronic mucocutaneous ulcerationYousef R Badran, Fatma Dedeoglu, Juan Manuel Leyva Castillo, et al.
The Journal of Allergy and Clinical Immunology|June 14, 2015
A novel mutation in ORAI1 presenting with combined immunodeficiency and residual T-cell functionJanet Chou, Yousef R Badran, Christina S K Yee, et al.
The Journal of Allergy and Clinical Immunology|May 20, 2019
Combined immunodeficiency in a patient with c-Rel deficiencySarah Beaussant-Cohen, Faris Jaber, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology|October 13, 2015
Autoimmune lymphoproliferative syndrome caused by a homozygous FasL mutation that disrupts FasL assemblyAli Sobh, Elena Crestani, Brittney Cangemi, et al.
Frontiers in Immunology|September 2, 2017
14 Years after Discovery: Clinical Follow-up on 15 Patients with Inducible Co-Stimulator DeficiencyJohanna Schepp, Janet Chou, Andrea Skrabl-Baumgartner, et al.
Clinical Immunology (Orlando, Fla.)|November 25, 2017
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delayVassilios Lougaris, Janet Chou, Manuela Baronio, et al.
Clinical Immunology (Orlando, Fla.)|November 25, 2019
Dysregulated actin dynamics in activated PI3Kδ syndromeJacqueline G Wallace, Pedro Zambrano-Rodas, Wilmer Córdova-Calderón, et al.
Pageof 16

Showing results (41-50 of 152) with videos related to

Sort By:
Pageof 16
Clinical Immunology (Orlando, Fla.)|August 20, 2016
Mutations in pyrin masquerading as a primary immunodeficiencyYousef R Badran, Mariam Rajab, Rima Hanna-Wakim, et al.
Clinical Immunology (Orlando, Fla.)|August 21, 2017
Combined immunodeficiency with EBV positive B cell lymphoma and epidermodysplasia verruciformis due to a novel homozygous mutation in RASGRP1Craig D Platt, Ari J Fried, Rodrigo Hoyos-Bachiloglu, et al.
Clinical Immunology (Orlando, Fla.)|April 12, 2016
Combined immunodeficiency due to a homozygous mutation in ORAI1 that deletes the C-terminus that interacts with STIM 1Yousef R Badran, Michel J Massaad, Wayne Bainter, et al.
The Journal of Experimental Medicine|June 11, 2017
Human <i>RELA</i> haploinsufficiency results in autosomal-dominant chronic mucocutaneous ulcerationYousef R Badran, Fatma Dedeoglu, Juan Manuel Leyva Castillo, et al.
The Journal of Allergy and Clinical Immunology|June 14, 2015
A novel mutation in ORAI1 presenting with combined immunodeficiency and residual T-cell functionJanet Chou, Yousef R Badran, Christina S K Yee, et al.
The Journal of Allergy and Clinical Immunology|May 20, 2019
Combined immunodeficiency in a patient with c-Rel deficiencySarah Beaussant-Cohen, Faris Jaber, Michel J Massaad, et al.
The Journal of Allergy and Clinical Immunology|October 13, 2015
Autoimmune lymphoproliferative syndrome caused by a homozygous FasL mutation that disrupts FasL assemblyAli Sobh, Elena Crestani, Brittney Cangemi, et al.
Frontiers in Immunology|September 2, 2017
14 Years after Discovery: Clinical Follow-up on 15 Patients with Inducible Co-Stimulator DeficiencyJohanna Schepp, Janet Chou, Andrea Skrabl-Baumgartner, et al.
Clinical Immunology (Orlando, Fla.)|November 25, 2017
Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delayVassilios Lougaris, Janet Chou, Manuela Baronio, et al.
Clinical Immunology (Orlando, Fla.)|November 25, 2019
Dysregulated actin dynamics in activated PI3Kδ syndromeJacqueline G Wallace, Pedro Zambrano-Rodas, Wilmer Córdova-Calderón, et al.
Pageof 16